Evidence map›Paper›PMID 26567478›Full record

ArticleAnnals of human genetics2016

The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions.

Michelle M Clark, John Blangero, Thomas D Dyer, Eric M Sobel, Janet S Sinsheimer

Open access · greenAbstract read
In one paragraph

Article in Annals of human genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Michelle M ClarkDepartment of Biostatistics, Fielding School of Public Health, University of California, Los Angeles, CA, USA.
John BlangeroSouth Texas Diabetes and Obesity Institute, School of Medicine, University of Texas, Rio Grande Valley, Brownsville, TX, USA.
Thomas D DyerSouth Texas Diabetes and Obesity Institute, School of Medicine, University of Texas, Rio Grande Valley, Brownsville, TX, USA.
Eric M SobelDepartment of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Janet S SinsheimerDepartment of Biostatistics, Fielding School of Public Health, University of California, Los Angeles, CA, USA.
Fielding Graduate University · USThe University of Texas Rio Grande Valley · USUniversity of California, Los Angeles · US

Funding

STATISTICAL METHODS FOR GENE MAPPINGR01GM053275 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LANGE, KENNETH L · 1995 to 2019
$9.3M
Training Grant in Genomic Analysis and InterpretationT32HG002536 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Valerie A Arboleda, Harold Pimentel · 2002 to 2026
$8.6M
Genomics, GPUs, and Next Generation Computational StatisticsR01HG006139 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SOBEL, ERIC · 2011 to 2023
$5.1M
NHGRI NIH HHS HG002536NHGRI NIH HHS HG006139NHGRI NIH HHS R01 HG006139NHGRI NIH HHS T32 HG002536NIGMS NIH HHS GM053275NIGMS NIH HHS R01 GM053275
6 · The paper itself

Abstract

Maternal-offspring gene interactions, aka maternal-fetal genotype (MFG) incompatibilities, are neglected in complex diseases and quantitative trait studies. They are implicated in birth to adult onset diseases but there are limited ways to investigate their influence on quantitative traits. We present the quantitative-MFG (QMFG) test, a linear mixed model where maternal and offspring genotypes are fixed effects and residual correlations between family members are random effects. The QMFG handles families of any size, common or general scenarios of MFG incompatibility, and additional covariates. We develop likelihood ratio tests (LRTs) and rapid score tests and show they provide correct inference. In addition, the LRT's alternative model provides unbiased parameter estimates. We show that testing the association of SNPs by fitting a standard model, which only considers the offspring genotypes, has very low power or can lead to incorrect conclusions. We also show that offspring genetic effects are missed if the MFG modeling assumptions are too restrictive. With genome-wide association study data from the San Antonio Family Heart Study, we demonstrate that the QMFG score test is an effective and rapid screening tool. The QMFG test therefore has important potential to identify pathways of complex diseases for which the genetic etiology remains to be discovered.

Indexed as

Genetic Predisposition to DiseaseGenotypeLinear ModelsModels, GeneticComputer SimulationFemaleGene FrequencyGenome-Wide Association StudyHumansLikelihood FunctionsPedigreePolymorphism, Single NucleotidePregnancyQuantitative Trait, Heritablefamily-based associationgene-gene interactionintergenerational effectsMaternal-fetal genotype incompatibilitymeasured genotype analysispedigree GWASquantitative traitsscore testvariance components

Identifiers

PMID26567478
PMCPMC4715557
OpenAlexW2216478888

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.